> ## Content Index
> Fetch the complete content index at: https://www.fdaweb.com/llms.txt
> Use this file to discover other available public pages before exploring further.

# Latest Federal Register Notices
- URL: https://www.fdaweb.com/latest-federal-register-notices-196/
- Published: 2018-09-23T12:00:00.000Z
- Updated: 2026-09-15T00:33:35.000Z
- Author: David McFarland
- Tags: Drugs, #legacy-id-D5142427

[**Joint Panel to Review Alkermes Depression NDA**](https://www.fdaweb.com/joint-panel-to-review-alkermes-depression-nda/)  
*Federal Register* notice: FDA announces an 11/1 joint advisory committee meeting to review an Alkermes NDA for major depressive disorder. 09/21/2018

[**Draft Guide on Clinicaltrials.com Money Penalties**](https://www.fdaweb.com/draft-guide-on-clinicaltrials-com-money-penalties/)  
*Federal Register* notice: FDA makes available a draft guidance entitled “Civil Money Penalties Relating to the ClinicalTrials.gov Data Bank; Draft Guidance for FDA Staff, Responsible Parties, and Submitters of Certain Applications and Submissions to FDA.” 09/21/2018

[**Guide on Product Identifier Requirements**](https://www.fdaweb.com/guide-on-product-identifier-requirements/)  
*Federal Register* notice: FDA makes available a final guidance entitled “Product Identifier Requirements Under the Drug Supply Chain Security Act— Compliance Policy.” 09/20/2018

[**Guide on Heparin Labeling and Safety Testing**](https://www.fdaweb.com/guide-on-heparin-labeling-and-safety-testing/)  
*Federal Register* notice: FDA makes available a final guidance entitled “Heparin-Containing Medical Devices and Combination Products: Recommendations for Labeling and Safety Testing.” 09/20/2018

[**Guide: Grandfathering Product Sans Product Identifier**](https://www.fdaweb.com/guide-grandfathering-product-sans-product-identifier/)  
*Federal Register* notice: FDA makes available a final guidance entitled “Grandfathering Policy for Packages and Homogenous Cases of Product Without a Product Identifier.” 09/20/2018

[**Q&A Guide on Product Identifiers**](https://www.fdaweb.com/q-a-guide-on-product-identifiers/)  
*Federal Register* notice: FDA makes available a draft guidance entitled “Product Identifiers Under the Drug Supply Chain Security Act Questions and Answers.” 09/20/2018

[**Docket Number Corrected on Post-approval Changes Guide**](https://www.fdaweb.com/docket-number-corrected-on-post-approval-changes-guide/)  
*Federal Register* notice: FDA corrects an incorrect docket number appearing in a 9/11 Federal Register notice entitled “Post-approval Changes to Drug Substances; Draft Guidance for Industry; Availability.” 09/19/2018

[**Comments Sought on Pediatric Safety Reviews**](https://www.fdaweb.com/comments-sought-on-pediatric-safety-reviews/)  
*Federal Register* notice: FDA establishes a public docket to collect comments related to the post-marketing, pediatric-focused safety reviews of products posted between 4/2 and 9/14 on FDA’s Web site. 09/18/2018